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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01385475
Other study ID # RTFunction
Secondary ID K01AG025962
Status Completed
Phase N/A
First received June 22, 2011
Last updated June 28, 2011
Start date June 2009
Est. completion date June 2011

Study information

Verified date June 2011
Source University of Wisconsin, Milwaukee
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The primary purpose of this study is to examine the effectiveness of the current resistance training guidelines for older adults proposed by ACSM/AHA to improve physical function in individuals with reduced physical abilities. A randomized controlled intervention trial will be used to compare change in physical function pre- and post-intervention between a treatment group receiving the minimum recommendations of the guidelines and a control group asked not to change their physical activity participation. To better understand the clinical significance of such an occurrence, a secondary purpose was to determine if older adults with reduced physical abilities who adhere to the recommended intervention dosage will experience a change such that they can be reclassified to a more favorable level of functioning. It is hypothesized that the minimum recommended dosage of the guidelines would be sufficient to both improve physical function and improve functional classification in older adults with reduced physical abilities.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date June 2011
Est. primary completion date December 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 65 Years to 90 Years
Eligibility Inclusion Criteria:

- Older Adults aged >65yrs; reduced physical function

Exclusion Criteria:

- Those with a history of resistance training

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
RT
8 week RT Intervention

Locations

Country Name City State
United States Physical Activity & Health Research Laboratory Milwaukee Wisconsin

Sponsors (2)

Lead Sponsor Collaborator
University of Wisconsin, Milwaukee National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Functionality Change in Short Performance Physical Battery (SPPB) score is used as a measure of functionality. The SPPB consists of three tasks designed to assess gait speed, and ability to rise from a chair and maintain standing balance. This is a common test to assess function, with scores ranging from 0-12. The higher score equates to a better level of function. 8 weeks No
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